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. Author manuscript; available in PMC: 2013 Sep 1.
Published in final edited form as: J Mol Cell Cardiol. 2012 Jun 6;53(3):446–457. doi: 10.1016/j.yjmcc.2012.05.018

Table 2.

Unloaded R193H and NTG myocyte contractile and Ca2+ transient parameters

Sarcomere Shortening Parameters
Resting SL (um) Shortening Amplitude (um) Dep Velocity (%amp) 50% Relaxation Time (s) 75% Relaxation Time (s) 90% Relaxation Time (s)
NTG 1.835±0.008 0.103±0.009 19.69±0.49 0.0689±0.002 0.107±0.004 0.18±0.01
R193H 1.675±0.01* 0.091±0.004 20.85±0.49 0.104±0.004* 0.209±0.008* 0.39±0.015*
Ca2+ Transient Parameters
Diastolic Ca2+ (360/380) Ca2+ Amplitude (360/380) Rise Velocity (%amp) 50% Decay Time (s) 75% Decay Time (s) 90% Decay Time (s)
NTG 1.14+0.02 0.115+0.012 87.7+8.6 0.141+0.004 0.266+0.012 0.42+0.03
R193H 0.09+0.02 0.055+0.004* 105.2+10.5 0.139+0.005 0.250+0.011 0.40+0.02

Departure and Ca2+ transient rise velocity is normalized to shortening and Ca2+ amplitude. Relaxation and Ca2+ decay time is calculated from peak shortening to 50, 75, or 90% of relaxation.

Values are represented as the mean ± SEM,

*

P<0.05 significantly different, t-test, n = 30 myocytes from 5 preparations.

Key: SL=Sarcomere Length, Dep Velocity = sarcomere length shortening velocity, and Rise Velocity = rate of rise of the Ca2+ transient.